| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.52676316C>G | CA16606335 | KRT1 | c.1434G>C (p.Glu478Asp) n.508G>C | ClinVar dbSNP |
| 12 | g.52676316C>A | CA217422 | KRT1 | c.1434G>T (p.Glu478Asp) n.508G>T | ClinVar dbSNP |
| 12 | g.52676316C= | CA2036619574 | KRT1 | c.1434G= (p.Glu478=) n.508G= | dbSNP dbSNP |
| 12 | g.52676316C>T | CA479872028 | KRT1 | c.1434G>A (p.Glu478=) n.508G>A | dbSNP |